Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormality of urine homeostasis (HP:0003110)

Parent Node:
Proteinuria (HP:0000093)

..Starting node
..Moderate proteinuria (HP:0012596)

Term ID:

12596

Name:

Moderate proteinuria

Synonym:

Definition:

Moderately increased levels of protein in the urine (500-1000 mg per day in adults).

Comments:

Reference:

HP:0012596

Genes and Diseases:

Child Nodes:

Sister Nodes:

Albuminuria (HP:0012592)

Bence Jones Proteinuria (HP:0030156)

Beta 2-microglobulinuria (HP:0025466)

Heavy proteinuria (HP:0012597)

Low-molecular-weight proteinuria (HP:0003126)

Mild proteinuria (HP:0012595)

Nephrotic range proteinuria (HP:0012593)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012596	HP:0012596	Moderate proteinuria	0	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.